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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1967 1
1968 4
1969 3
1970 1
1971 1
1973 2
1974 2
1977 3
1978 4
1979 4
1980 5
1981 2
1982 3
1983 3
1984 1
1985 3
1986 3
1987 4
1988 7
1989 11
1990 1
1991 7
1992 9
1993 7
1994 2
1995 6
1996 7
1997 7
1998 6
1999 10
2000 8
2001 11
2002 19
2003 10
2004 11
2005 12
2006 12
2007 16
2008 24
2009 30
2010 19
2011 24
2012 31
2013 30
2014 22
2015 38
2016 37
2017 37
2018 37
2019 39
2020 37
2021 34
2022 39
2023 40
2024 33
2025 33

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720 results

Results by year

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Page 1
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients.
Borràs N, Batlle J, Pérez-Rodríguez A, López-Fernández MF, Rodríguez-Trillo Á, Lourés E, Cid AR, Bonanad S, Cabrera N, Moret A, Parra R, Mingot-Castellano ME, Balda I, Altisent C, Pérez-Montes R, Fisac RM, Iruín G, Herrero S, Soto I, de Rueda B, Jiménez-Yuste V, Alonso N, Vilariño D, Arija O, Campos R, Paloma MJ, Bermejo N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Sarmiento L, Iñigo B, Nieto MDM, Vidal R, Martínez MP, Aguinaco R, César JM, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Cornudella R, Aguilar C, Vidal F, Corrales I. Borràs N, et al. Among authors: marco p. Haematologica. 2017 Dec;102(12):2005-2014. doi: 10.3324/haematol.2017.168765. Epub 2017 Sep 29. Haematologica. 2017. PMID: 28971901 Free PMC article.
Neuroblastoma Patients' Outcome and Chromosomal Instability.
Ognibene M, De Marco P, Amoroso L, Fragola M, Zara F, Parodi S, Pezzolo A. Ognibene M, et al. Among authors: de marco p. Int J Mol Sci. 2023 Oct 24;24(21):15514. doi: 10.3390/ijms242115514. Int J Mol Sci. 2023. PMID: 37958497 Free PMC article.
Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder.
Accogli A, Park YN, Lenk GM, Severino M, Scala M, Denecke J, Hempel M, Lessel D, Kortüm F, Salpietro V, de Marco P, Guerrisi S, Torella A, Nigro V, Srour M, Turro E, Labarque V, Freson K, Piatelli G, Capra V, Kitzman JO, Meisler MH. Accogli A, et al. Among authors: de marco p. Genet Med. 2024 May;26(5):101097. doi: 10.1016/j.gim.2024.101097. Epub 2024 Feb 5. Genet Med. 2024. PMID: 38334070 Free article.
Chiari malformation type I: what information from the genetics?
Capra V, Iacomino M, Accogli A, Pavanello M, Zara F, Cama A, De Marco P. Capra V, et al. Among authors: de marco p. Childs Nerv Syst. 2019 Oct;35(10):1665-1671. doi: 10.1007/s00381-019-04322-w. Epub 2019 Aug 5. Childs Nerv Syst. 2019. PMID: 31385087 Review.
Dual-phase amyloid PET: hitting two birds with one stone.
Valentina G, Silvia M, Marco P. Valentina G, et al. Among authors: marco p. Eur J Nucl Med Mol Imaging. 2016 Jul;43(7):1300-3. doi: 10.1007/s00259-016-3393-6. Epub 2016 Apr 23. Eur J Nucl Med Mol Imaging. 2016. PMID: 27105874 No abstract available.
Evaluating hazardous air pollutants in Australia.
Hinwood AL, Di Marco PN. Hinwood AL, et al. Among authors: di marco pn. Toxicology. 2002 Dec 27;181-182:361-6. doi: 10.1016/s0300-483x(02)00466-3. Toxicology. 2002. PMID: 12505337 Review.
720 results